Altered apolipoprotein A-V expression during the acute phase response is independent of plasma triglyceride levels in mice and humans

被引:13
作者
Becker, S
Schomburg, L
Renko, K
Tölle, M
van der Giet, M
Tietge, UJF
机构
[1] Dept Med, Berlin, Germany
[2] Inst Expt Endocrinol, Berlin, Germany
[3] Med Klin 4, Berlin, Germany
[4] Univ Groningen, Med Ctr, Ctr Liver Disgest & Metab Dis, Groningen, Netherlands
关键词
metabolism; inflammation; lipoproteins; cytokines; regulation;
D O I
10.1016/j.bbrc.2005.11.105
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Plasma triglyceride (TG) levels are altered during the acute phase response (APR). Plasma levels of the recently discovered apolipoprotein AN (apoA-V) are inversely associated with plasma TG. The aim of this study was to investigate the change of apoA-V plasma levels and hepatic apoA-V expression during the APR in relation to plasma TG. During human APR plasma apoA-V was decreased as were plasma TG (each P < 0.01). Also early in the course of the murine APR plasma apoA-V levels and hepatic apoA-V expression were decreased and changed in the same direction as plasma TG. Treatment of HepG2 cells with TNF-alpha and IL-1 beta decreased apoA-V mRNA levels early by 42% and 55%, respectively (each P < 0.001). However, in promoter/reporter assays the human apoA-V promoter was unresponsive to proinflammatory cytokines. Instead, we demonstrate that a significant decrease in apoA-V mRNA stability in response to treatment with TNF-alpha and IL-1 beta is the underlying basis of decreased apoA-V expression during the APR (P < 0.05). These data demonstrate that (i) apoA-V expression decreases early during the APR due to changes in mRNA stability, and (ii) during the APR apoA-V is not inversely related to plasma TG levels in mice and humans, thereby identifying a relevant pathophysiological setting, in which the previously reported close inverse association between these parameters does not hold true. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:833 / 839
页数:7
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